Evidence map›Paper›PMID 35577330›Full record

ArticleNeurospine2022

Recent Molecular and Genetic Findings in Intramedullary Spinal Cord Tumors.

Yoshitaka Nagashima, Yusuke Nishimura, Kaoru Eguchi, Junya Yamaguchi, Shoichi Haimoto, Fumiharu Ohka, Masakazu Takayasu, Ryuta Saito

Abstract read
In one paragraph

Article in Neurospine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Yoshitaka NagashimaDepartment of Neurosurgery, Nagoya University School of Medicine, Nagoya, Japan.
Yusuke NishimuraDepartment of Neurosurgery, Nagoya University School of Medicine, Nagoya, Japan.
Kaoru EguchiDepartment of Neurosurgery, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Junya YamaguchiDepartment of Neurosurgery, Nagoya University School of Medicine, Nagoya, Japan.
Shoichi HaimotoDepartment of Neurosurgery, Aichi Cancer Center Hospital, Nagoya, Japan.
Fumiharu OhkaDepartment of Neurosurgery, Nagoya University School of Medicine, Nagoya, Japan.
Masakazu TakayasuDepartment of Neurosurgery, Inazawa Municipal Hospital, Aichi, Japan.
Ryuta SaitoDepartment of Neurosurgery, Nagoya University School of Medicine, Nagoya, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The study of genetic alterations and molecular biology in central nervous system (CNS) tumors has improved the accuracy of estimations of patient prognosis and tumor categorization. Therefore, the updated 2021 World Health Organization (WHO) classification includes various diagnostic genes, molecules, and pathways for diagnosis, as well as histological findings. These findings are expected both to have diagnostic applications and to facilitate new targeted therapies that target tumor-specific genetic changes and molecular biology. Intramedullary spinal cord tumors (IMSCTs) are rare CNS tumors that are difficult to treat because they occur in eloquent areas. Although the genetic underpinnings of IMSCTs remain unclear compared to their intracranial counterparts, the genetic characteristics of these tumors are gradually being revealed. Here, we describe the major changes in the new 2021 WHO classification and review the major types of IMSCTs, with an emphasis on their clinical features and genetic alterations.

Indexed as

AstrocytomaEpendymomaGeneticsGenomicsHemangioblastomaIntramedullary spinal cord tumor

Identifiers

PMID35577330
PMCPMC9260550

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.